narcan

Generic: naloxone hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name narcan
Generic Name naloxone hydrochloride
Labeler a-s medication solutions
Dosage Form SPRAY
Routes
NASAL
Active Ingredients

naloxone hydrochloride 4 mg/.1mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2422
Product ID 50090-2422_caf3eabb-89bd-469a-9d00-3fd3a18fb5db
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA208411
Listing Expiration 2026-12-31
Marketing Start 2017-01-24

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902422
Hyphenated Format 50090-2422

Supplemental Identifiers

RxCUI
1725059 1725064
UNII
F850569PQR

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name narcan (source: ndc)
Generic Name naloxone hydrochloride (source: ndc)
Application Number NDA208411 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/.1mL
source: ndc
Packaging
  • 2 VIAL, SINGLE-DOSE in 1 PACKAGE (50090-2422-0) / .1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

naloxone hydrochloride (4 mg/.1mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "caf3eabb-89bd-469a-9d00-3fd3a18fb5db", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059", "1725064"], "spl_set_id": ["139c30b9-5600-48f5-8610-0cacd2782398"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 PACKAGE (50090-2422-0)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50090-2422-0", "marketing_start_date": "20170124"}], "brand_name": "NARCAN", "product_id": "50090-2422_caf3eabb-89bd-469a-9d00-3fd3a18fb5db", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-2422", "generic_name": "Naloxone Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NARCAN", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "NDA208411", "marketing_category": "NDA", "marketing_start_date": "20170124", "listing_expiration_date": "20261231"}